510(k) K935791 ยท ESD Hearing Aid, Air-Conduction, Prescription
PHONAK PICONET 232X-AZ BTE HEARING INSTRUMENT
| Applicant | Phonak, Inc., Naperville IL, US |
| Decision | Substantially Equivalent, Jan 26, 1994 |
| Received | Dec 7, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935791
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.